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jaxons_kingdom
Jaxon’s Kingdom was created in loving memory of our son, Jaxon, who passed away in August 2024 at just 16 years old from Sanfilippo Syndrome (MPS).
Sanfilippo is a terminal genetic condition that affects the entire body, causing cognitive decline, loss of speech, seizures, and ultimately a shortened life expectancy. There is currently no cure or approved treatment.
Through Jaxon’s Kingdom, we are committed to raising awareness, honoring Jaxon’s life, and fighting for a future where no family has to endure this diagnosis. We refuse to let his story end here. Help us spread awareness and support the search for a cure.
Learn more or support the mission at www.curesanfilippofoundation.org1.4K following
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